The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126650281 12665028 1 I 20151130 20160818 20160818 PER US-BAUSCH-BL-2015-029007 BAUSCH AND LOMB 0.00 F Y 62.65000 KG 20160818 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126650281 12665028 1 PS ZEGERID OMEPRAZOLESODIUM BICARBONATE 1 Oral 21636 ORAL SUSPENSION
126650281 12665028 2 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown 0
126650281 12665028 3 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown 0
126650281 12665028 4 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126650281 12665028 1 Product used for unknown indication
126650281 12665028 2 Product used for unknown indication
126650281 12665028 3 Product used for unknown indication
126650281 12665028 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126650281 12665028 Abdominal distension
126650281 12665028 Drug ineffective
126650281 12665028 Urticaria
126650281 12665028 Weight increased
126650281 12665028 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126650281 12665028 4 1997 1999 0